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For synthtic application see: (b) Williams, D. R.; Lowder, P. D.; Gu, Y.-G.; Brooks, D. A. Tetrahedron Lett. 1997, 38, 331. (c) Freeman, D. J.; Pattenden, G. Tetrahedron Lett. 1998, 39, 3251. (d) Pattenden, G.; Thompson, T. Chem. Commun. 2001, 8, 717. (e) Yokokawa, F.; Sameshima, H.; Shioiri, T. Tetrahedron Lett. 2001, 42, 4171.
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Williams, D.R.1
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7
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0032516335
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For synthtic application see: (b) Williams, D. R.; Lowder, P. D.; Gu, Y.-G.; Brooks, D. A. Tetrahedron Lett. 1997, 38, 331. (c) Freeman, D. J.; Pattenden, G. Tetrahedron Lett. 1998, 39, 3251. (d) Pattenden, G.; Thompson, T. Chem. Commun. 2001, 8, 717. (e) Yokokawa, F.; Sameshima, H.; Shioiri, T. Tetrahedron Lett. 2001, 42, 4171.
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Freeman, D.J.1
Pattenden, G.2
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8
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0035926097
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For synthtic application see: (b) Williams, D. R.; Lowder, P. D.; Gu, Y.-G.; Brooks, D. A. Tetrahedron Lett. 1997, 38, 331. (c) Freeman, D. J.; Pattenden, G. Tetrahedron Lett. 1998, 39, 3251. (d) Pattenden, G.; Thompson, T. Chem. Commun. 2001, 8, 717. (e) Yokokawa, F.; Sameshima, H.; Shioiri, T. Tetrahedron Lett. 2001, 42, 4171.
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Pattenden, G.1
Thompson, T.2
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9
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0035908266
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For synthtic application see: (b) Williams, D. R.; Lowder, P. D.; Gu, Y.-G.; Brooks, D. A. Tetrahedron Lett. 1997, 38, 331. (c) Freeman, D. J.; Pattenden, G. Tetrahedron Lett. 1998, 39, 3251. (d) Pattenden, G.; Thompson, T. Chem. Commun. 2001, 8, 717. (e) Yokokawa, F.; Sameshima, H.; Shioiri, T. Tetrahedron Lett. 2001, 42, 4171.
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Yokokawa, F.1
Sameshima, H.2
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Akita, H.; Kato, K.; Nishimura, A.; Yamamoto, Y. Tetrahedron Lett. 2002, 43, 643.
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Akita, H.1
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Manuscript in preparation
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Charette, A. B.; DeRoy, P. L.; Berthelette, C.; Lacombe, P.; Sametz, G. Manuscript in preparation.
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0033518561
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For a general procedure of the Z or E silylketene acetal see: Evans, D. A.; Kozlowski, M. C.; Murry, J. A.; Burgey, C. S.; Connell, B. T. J. Am. Chem. Soc. 1999, 121, 669.
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(a) Meerwein, H.; Laasch, P.; Mersch, R.; Spille, J. Chem. Ber. 1956, 89, 203.
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0028001763
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(b) Pettit, G. R.; Singh, S. B.; Herald, D. L.; Lloyd-Williams, P.; Kantoci, D.; Burkett, D. D.; Barkoczy, J.; Hogan, F.; Wardlaw, T. R. J. Org. Chem. 1994, 59, 6287.
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Barkoczy, J.7
Hogan, F.8
Wardlaw, T.R.9
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19
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0036277649
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For synthetic application see: (a) Tokuyama, H.; Yokoshima, S.; Lin, S.-C.; Li, L.; Fukuyama, T. Synthesis 2002, 8, 1121. (b) Fukuyama, T.; Lin, S.-C.; Li, L. J. Am. Chem. Soc. 1990, 19, 7050. (c) Kanda, Y.; Fukuyama, T. J. Am. Chem. Soc. 1993, 115, 8451.
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Synthesis
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Tokuyama, H.1
Yokoshima, S.2
Lin, S.-C.3
Li, L.4
Fukuyama, T.5
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20
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0025073031
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For synthetic application see: (a) Tokuyama, H.; Yokoshima, S.; Lin, S.-C.; Li, L.; Fukuyama, T. Synthesis 2002, 8, 1121. (b) Fukuyama, T.; Lin, S.-C.; Li, L. J. Am. Chem. Soc. 1990, 19, 7050. (c) Kanda, Y.; Fukuyama, T. J. Am. Chem. Soc. 1993, 115, 8451.
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Fukuyama, T.1
Lin, S.-C.2
Li, L.3
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21
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0027493927
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-
For synthetic application see: (a) Tokuyama, H.; Yokoshima, S.; Lin, S.-C.; Li, L.; Fukuyama, T. Synthesis 2002, 8, 1121. (b) Fukuyama, T.; Lin, S.-C.; Li, L. J. Am. Chem. Soc. 1990, 19, 7050. (c) Kanda, Y.; Fukuyama, T. J. Am. Chem. Soc. 1993, 115, 8451.
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Kanda, Y.1
Fukuyama, T.2
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22
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0001356803
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Wiley: New York, Collect.
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(a) The methyldiazoacetate was prepared as described in: Womack, E. B.; Nelson, A. B. Organic Syntheses; Wiley: New York, 1955; Collect. Vol. III, p. 392.
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(1955)
Organic Syntheses
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Womack, E.B.1
Nelson, A.B.2
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23
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0033546338
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(b) For synthetic application, see: Yajura, T.; Ueki, A.; Kitamura, T.; Tanaka, K.; Nameki, M.; Ikeda, M. Tetrahedron 1999, 55, 7461.
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(1999)
Tetrahedron
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Yajura, T.1
Ueki, A.2
Kitamura, T.3
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Nameki, M.5
Ikeda, M.6
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24
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0031825110
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(c) Yakura, T.; Yuamada, S.; Azuma, M.; Ueki, A.; Ikeda, M. Synthesis 1998, 7, 973.
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Synthesis
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Yakura, T.1
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Ikeda, M.5
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25
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0033546338
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(d) Yakura, T.; Ueki, A.; Kitamura, T.; Tanaka, K.; Nameki, M.; Ikeda, M. Tetrahedron 1999, 55, 7461.
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Yakura, T.1
Ueki, A.2
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Nameki, M.5
Ikeda, M.6
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26
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0002732797
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(e) Phukan, P.; Mohan, J. M.; Sudalai, A. J. Chem. Soc., Perkin Trans. 1 1999, 24, 3685.
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J. Chem. Soc., Perkin Trans. 1
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Phukan, P.1
Mohan, J.M.2
Sudalai, A.3
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30
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0345124335
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NMR spectra are identical to those reported: see ref 4a
-
NMR spectra are identical to those reported: see ref 4a.
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-
-
-
31
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0344693635
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note
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Thiazoline prepared from 18 was not purified since it partially oxidized on silica gel.
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32
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0034684178
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Evans, D. A.; Fitch, D. M.; Smith, T. E.; Victor, J. C. J. Am. Chem. Soc. 2000, 122, 10033.
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(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 10033
-
-
Evans, D.A.1
Fitch, D.M.2
Smith, T.E.3
Victor, J.C.4
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